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Clinical Trials/KCT0002451
KCT0002451
Recruiting
未知

Investigation on the Effects of Acupuncture on Cognitive improvement in patients with Mild Cognitve Impairment using f-NIRS

Dunsan Korean Medicine Hospital of Daejeon University0 sites24 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Dunsan Korean Medicine Hospital of Daejeon University
Enrollment
24
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Dunsan Korean Medicine Hospital of Daejeon University

Eligibility Criteria

Inclusion Criteria

  • 1\. Aged from equal to or more than 45 to under 80 years old
  • 2\. Understand the purpose of the study and agree to participate
  • \<Experimental group\>
  • 1\. Patients who meet the Peterson diagnostic criteria of mild cognitive impairment (MCI) with memory problems at least for 3 months
  • 2\. At least 6 years of education
  • 3\. Hachinski ischemic score \= 6
  • 4\. Korean Montreal Cognitive Assessment (MoCA\-K) score \= 22
  • 5\. Clinical dementia rating score 0\.5 AND global deterioration scale score 2\-3
  • \<Normal control group\>
  • 1\. Korean Montreal Cognitive Assessment (MoCA\-K) score \=23

Exclusion Criteria

  • 1\. Dementia by Diagnostic and Statistical Manual of Mental Disorders\-IV (DSM\-IV)
  • 2\. History of neurological disorder that can cause cognitive decline (Parkinson's disease, stroke, cerebral hemorrhage, tumors, normal pressure hydrocephalus, etc.)
  • 3\. Received any treatment for MCI during the past 4 weeks
  • 4\. Patients who were involved in other clinical trials within 4 weeks
  • 5\. Those who have experienced hypersensitivity reactions after acupuncture treatment, or who are difficult to cooperate with acupuncture treatment
  • 6\. A patient who is likely to have a non\-cooperative attitude in this clinical study or who is judged by the researcher to be unable to proceed with the study
  • 7\. Those who can not measure f\-NIRS

Outcomes

Primary Outcomes

Not specified

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